NEBIVOLOL
- Product NDC
- 63629-9589
- 11-digit product format
- 636299589
- Labeler code
- 63629
- Product ID
- 63629-9589_3d65f7e0-9bf7-40e1-8744-a626c749b572
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nebivolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212682
- Marketing category
- ANDA
- Marketing start
- 2022-02-14
- Substance
- NEBIVOLOL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- NEBIVOLOL
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NEBIVOLOL | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 030Y90569U |
| Rxcui | 387013 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-9589-1 | NEBIVOLOL | 90 in 1 BOTTLE | TABLET | 90 | | 103 |
| 63629-9589-2 | NEBIVOLOL | 30 in 1 BOTTLE | TABLET | 30 | | 103 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-9589 | NEBIVOLOL TABLET [BRYANT RANCH PREPACK] | 103 | Current NDC, Legacy NDC, 2 package rows | 20240726_77fb6b5f-7bfe-4fc8-980c-fc688ac9837a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-9589-1 | 63629958901 | 90 TABLET in 1 BOTTLE (63629-9589-1) | 90 tablet | 2022-12-01 | 0000-00-00 | No | No | Current |
| 63629-9589-2 | 63629958902 | 30 TABLET in 1 BOTTLE (63629-9589-2) | 30 tablet | 2022-12-01 | | No | No | Current |